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Sweroside Alleviated LPS-Induced Inflammation via SIRT1 Mediating NF-κB and FOXO1 Signaling Pathways in RAW264.7 Cells

机译:Sweroside通过SIRT1介导RAW264.7细胞中NF-κB和FOXO1信号通路减轻LPS诱导的炎症

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摘要

Pterocephalus hookeri was used as a traditional Chinese medicine for the treatment of rheumatoid arthritis. Sweroside was a main iridoid isolated from P. hookeri. The present study aimed to investigate the anti-inflammatory effect mechanism of sweroside. In RAW264.7 cells induced by lipopolysaccharide (LPS), the abnormal proliferation, the NO content increase, and the downregulated Sirtuin1 (SIRT1) expression were observed. Sweroside could alleviate the inflammation by inhibiting cell proliferation through arresting the cell cycle at the G0/G1 phase, by suppressing pro-inflammatory cytokines and by promoting anti-inflammatory cytokines in LPS-induced RAW264.7 cells. Further mechanism research indicated that sweroside could activate the SIRT1, then suppress the nuclear factor-kappa B (NF-κB) and promote the Forkhead transcription factor O1 (FOXO1) signaling pathways. The present study indicated that sweroside may be the main anti-inflammatory constituent of P. hookeri and a promising candidate for anti-inflammation therapy.
机译:钩端螺旋体被用作治疗类风湿关节炎的中药。 Sweroside是分离自P. hookeri的一种主要虹彩。本研究旨在探讨苦参碱的抗炎作用机理。在脂多糖(LPS)诱导的RAW264.7细胞中,观察到异常增殖,NO含量增加和Sirtuin1(SIRT1)表达下调。 Sweroside可以通过在G0 / G1期阻滞细胞周期,抑制促炎细胞因子和促进LPS诱导的RAW264.7细胞中的抗炎细胞因子来抑制细胞增殖来减轻炎症。进一步的机制研究表明,苦参甙可以激活SIRT1,然后抑制核因子-κB(NF-κB)并促进Forkhead转录因子O1(FOXO1)信号通路。本研究表明,苦参甙可能是钩端螺旋体的主要抗炎成分,也是抗炎治疗的有希望的候选者。

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